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Sulfuric Acid → HCID 59797078、化合物

HRID 34019
ノート
印刷プレビュー

反応式

HRID 34019 の反応式
[F:1][C:2]1[CH:10]=[C:9]2[C:5]([C:6](/[CH:11]=[CH:12]/[C:13]3[CH:18]=[CH:17][CH:16]=[C:15]([F:19])[CH:14]=3)=[N:7][NH:8]2)=[CH:4][C:3]=1[C:20]#[N:21].S(=O)(=O)(O)[OH:23]>C(O)(=O)C.O>[F:1][C:2]1[CH:10]=[C:9]2[C:5]([C:6](/[CH:11]=[CH:12]/[C:13]3[CH:18]=[CH:17][CH:16]=[C:15]([F:19])[CH:14]=3)=[N:7][NH:8]2)=[CH:4][C:3]=1[C:20]([NH2:21])=[O:23]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 1118Sulfuric AcidHCID 59797063HCID 59797063、化合物

生成物 1

HCID 59797078HCID 59797078、化合物

試薬・触媒・溶媒 2

HCID 176Acetic Acid溶媒HCID 962Water溶媒

反応条件

温度
110 °C

実験手順

To a suspension of 89 mg of 6-fluoro-3-[(E)-2-(3-fluorophenyl)-vinyl]-1H-indazole-5-carbonitrile obtained by Example 100 in 0.4 mL of acetic acid and 0.4 mL of water was added 1.2 mL of concentrated sulfuric acid, and stirred at 110° C. for 50 minutes. After allowing to cool, ice was added, and extracted with a mixed solvent of 20 mL of ethyl acetate and 10 mL of tetrahydrofuran. The organic layer was washed successively with water, saturated aqueous sodium hydrogen carbonate and saturated brine, and dried over anhydrous magnesium sulfate. After making the organic layer pass through an alumina pad (2.5 diameter ×2 cm), the solvent was evaporated, to afford 76 mg of the title compound as pale yellow crystals.

後処理

  1. temperatureto cool
  2. additionice was added
  3. extractionextracted with a mixed solvent of 20 mL of ethyl acetate and 10 mL of tetrahydrofuran
  4. washThe organic layer was washed successively with water, saturated aqueous sodium hydrogen carbonate and saturated brine
  5. dry with materialdried over anhydrous magnesium sulfate
  6. customthe solvent was evaporated

出典と根拠

ORDレコード
ord-ec5d1b48389d430c827dd05007c46d52
出典データセット
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07429609B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート